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    Didanosine

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    Aspen Pharmacare Holdings

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    Didanosine

    Brand Name : Aspen Didanosine

    Dosage Form : TAB

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    Didanosine

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    Barr Laboratories

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    DIDANOSINE

    Brand Name : DIDANOSINE

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 200MG

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    Approval Date : 2004-12-03

    Application Number : 77167

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    Registration Country : USA

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    DIDANOSINE

    Brand Name : DIDANOSINE

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 250MG

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    Approval Date : 2004-12-03

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    Bristol Laboratories Ltd

    United Kingdom
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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 10MG/ML

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    Approval Date : 1991-10-09

    Application Number : 20156

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    Bristol Myers Squibb

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-10-09

    Application Number : 20154

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    Registration Country : USA

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-10-09

    Application Number : 20154

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    Bristol Myers Squibb

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-10-09

    Application Number : 20154

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    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-10-09

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    Bristol Myers Squibb

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1999-10-28

    Application Number : 20154

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    Bristol Myers Squibb

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 100MG/PACKET

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    Approval Date : 1991-10-09

    Application Number : 20155

    Regulatory Info : DISCN

    Registration Country : USA

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    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 167MG/PACKET

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    Approval Date : 1991-10-09

    Application Number : 20155

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 250MG/PACKET

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    Approval Date : 1991-10-09

    Application Number : 20155

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    DIDANOSINE

    Brand Name : VIDEX

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 375MG/PACKET

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    Approval Date : 1991-10-09

    Application Number : 20155

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    DIDANOSINE

    Brand Name : VIDEX EC

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-10-31

    Application Number : 21183

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    Brand Name : VIDEX EC

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-10-31

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    Brand Name : VIDEX EC

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-10-31

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    DIDANOSINE

    Brand Name : VIDEX EC

    Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

    Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-10-31

    Application Number : 21183

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